510(k) K790514
- Device
- I Netilmicin Ria Kit
- Applicant
- DIAGNOSTIC PRODUCTS CORP.
- 510(k) number
- K790514
- Product code
- JTB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-05-03
- Date received
- 1979-03-15
- Regulation
- 866.2440
- Classification name
- Device, Media Dispensing/Stacking
- Medical specialty
- Microbiology
- Review panel
- Microbiology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3018125942
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code JTB#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K802561 | HI VOLUME PUMPING CHAMBER | Acacia, Inc. | 1980-10-31 |